RFLPs at the low-density lipoprotein (LDL) receptor locus for TaqI, StuI, HincII, AvaII, ApaLI (5` and 3`), PvuII, and NcoI were studied in Swiss and German families with familial hypercholesterolemia (FH). A total of 1,104 LDL receptor alleles were analyzed using Southern blotting and new PCR-based techniques for detection of the TaqI, StuI, HincII, AvaII, NcoI RFLPs. Two hundred fifty-six independent haplotypes from 368 individuals of 61 unrelated Swiss families, as well as 114 independent haplotypes from 184 subjects of 25 unrelated German families, were constructed. In 76 families, clinical diagnosis of FH was confirmed by cosegregation analysis. Of the 43 unique haplotypes consisting of seven RFLPs detected in the Swiss and Germans, on...
Aims We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and c...
From a large cohort of hyperlipidemic patients, who attended the Lipid Research Clinic in Amsterdam,...
In most patients with heterozygous familial hypercholesterolaemia (FH) the disorder is caused by a m...
Familial hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal dominant trait ...
Many low-density lipoprotein (LDL) receptor mutations have been identified and characterized, demons...
The aim of this study was the characterization of mutations of the LDL receptor gene in 39 Italian p...
Seventy-one mutations of the low density lipoprotein (LDL) receptor gene were identified in 282 unre...
We studied the association between common haplotypes in six relevant lipid metabolism genes with pla...
To investigate the molecular basis of familial hypercholesterolemia (FH) in France, we applied the s...
Seventy-one mutations of the low density lipoprotein (LDL) receptor gene were identified in 282 unre...
AbstractA cDNA probe for the low density lipoprotein (LDL) receptor gene was used to screen DNA samp...
Abstract A large number of rare mutations in the low-density lipoprotein (LDL) receptor gene cause t...
We have used four restriction fragment length polymorphisms (RFLPs) of the human low density lipopro...
Familial hypercholesterolemia (FH) is one of the most common autosomal codominant diseases. FH is ca...
Mutations in the LDL receptor are responsible for familial hypercholesterolemia (FH). At present, mo...
Aims We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and c...
From a large cohort of hyperlipidemic patients, who attended the Lipid Research Clinic in Amsterdam,...
In most patients with heterozygous familial hypercholesterolaemia (FH) the disorder is caused by a m...
Familial hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal dominant trait ...
Many low-density lipoprotein (LDL) receptor mutations have been identified and characterized, demons...
The aim of this study was the characterization of mutations of the LDL receptor gene in 39 Italian p...
Seventy-one mutations of the low density lipoprotein (LDL) receptor gene were identified in 282 unre...
We studied the association between common haplotypes in six relevant lipid metabolism genes with pla...
To investigate the molecular basis of familial hypercholesterolemia (FH) in France, we applied the s...
Seventy-one mutations of the low density lipoprotein (LDL) receptor gene were identified in 282 unre...
AbstractA cDNA probe for the low density lipoprotein (LDL) receptor gene was used to screen DNA samp...
Abstract A large number of rare mutations in the low-density lipoprotein (LDL) receptor gene cause t...
We have used four restriction fragment length polymorphisms (RFLPs) of the human low density lipopro...
Familial hypercholesterolemia (FH) is one of the most common autosomal codominant diseases. FH is ca...
Mutations in the LDL receptor are responsible for familial hypercholesterolemia (FH). At present, mo...
Aims We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and c...
From a large cohort of hyperlipidemic patients, who attended the Lipid Research Clinic in Amsterdam,...
In most patients with heterozygous familial hypercholesterolaemia (FH) the disorder is caused by a m...